RS61754370 TYR

Health Risk Chr 11:89178719
Upload your DNA to see your genotype for this variant.
Associated Conditions
Inborn genetic diseases
Oculocutaneous albinism type 1A
Oculocutaneous albinism type 1B
Inborn genetic diseases
Oculocutaneous albinism type 1A
Oculocutaneous albinism type 1B
Other Variants in TYR
rs281865527 rs28940876 rs104894314 rs61754388 rs121908011 rs61753185 rs104894313 rs1042602 rs1126809 rs28940877
Ask Dr. Hemsworth about this variant